Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Bunkyo City, Japan.
Department of Cell Therapy and Transplantation Medicine, The University of Tokyo Hospital, Bunkyo City, Japan.
Transpl Infect Dis. 2020 Dec;22(6):e13433. doi: 10.1111/tid.13433. Epub 2020 Aug 10.
BK polyomavirus (BKV) causes two distinct complications after transplantation, hemorrhagic cystitis (BKV-HC) after hematopoietic stem cell transplantation (HSCT), and BKV-associated nephropathy (BKVAN) after kidney transplantation (KT). Although fluoroquinolones show efficacy against BKV proliferation in vitro, the clinical effect remains uncertain; thus, we performed meta-analysis to assess its efficacy in the prophylaxis.
Articles published before March 2020 were searched from PubMed, the Cochrane Library, ISRCTN registry, and ClinicalTrials.gov. Primary outcomes were BKV-HC after HSCT and BKVAN after KT. Secondary outcomes were BK viremia, viruria after KT, and fluoroquinolone-related adverse events.
Three trials with 281 patients post-HSCT and 11 trials with 1882 patients post KT were included as for prophylaxis. Fluoroquinolone prophylaxis did not show effects on BKV-HC (OR 0.54, 95% CI 0.13-2.25), BKVAN (OR 0.74, 95% CI 0.35-1.55), and BK viremia (OR 0.79, 95% CI 0.49-1.28), but significantly decreased BK viruria (OR 0.64, 95% CI 0.45-0.91). Fluoroquinolone prophylaxis was associated with the higher percentage of fluoroquinolone-resistant infection among identified bacteria (OR 2.38, 95% CI 1.16-4.88), but the incidence of fluoroquinolone-resistant infection was similar (OR 1.15, 95% CI 0.71-1.86), due to the decrease of infection itself (OR 0.52, 95% CI 0.34-0.81).
This meta-analysis showed that fluoroquinolones did not prevent BKV-HC after HSCT or BKVAN after KT, although the effect against BKV-HC should be further investigated by randomized controlled trials. Fluoroquinolones could reduce the rate of BK viruria to some extent but may not have clinically sufficient effects.
BK 多瘤病毒(BKV)在移植后会引起两种不同的并发症,造血干细胞移植(HSCT)后发生出血性膀胱炎(BKV-HC),肾移植(KT)后发生 BKV 相关性肾病(BKVAN)。尽管氟喹诺酮类药物在体外显示出对 BKV 增殖的疗效,但临床效果仍不确定;因此,我们进行了荟萃分析以评估其在预防中的疗效。
检索了 2020 年 3 月之前发表的来自 PubMed、Cochrane 图书馆、ISRCTN 注册处和 ClinicalTrials.gov 的文章。主要结局是 HSCT 后 BKV-HC 和 KT 后 BKVAN。次要结局是 BK 血症、KT 后尿病毒血症和氟喹诺酮类相关不良事件。
有 3 项 HSCT 后 281 例患者和 11 项 KT 后 1882 例患者的试验被纳入预防措施。氟喹诺酮类预防措施对 BKV-HC(OR 0.54,95%CI 0.13-2.25)、BKVAN(OR 0.74,95%CI 0.35-1.55)和 BK 血症(OR 0.79,95%CI 0.49-1.28)无影响,但显著降低了 BK 尿病毒血症(OR 0.64,95%CI 0.45-0.91)。氟喹诺酮类预防与已鉴定细菌中氟喹诺酮类耐药感染的百分比较高有关(OR 2.38,95%CI 1.16-4.88),但氟喹诺酮类耐药感染的发生率相似(OR 1.15,95%CI 0.71-1.86),这是由于感染本身的减少(OR 0.52,95%CI 0.34-0.81)。
这项荟萃分析表明,氟喹诺酮类药物不能预防 HSCT 后 BKV-HC 或 KT 后 BKVAN,尽管需要通过随机对照试验进一步研究氟喹诺酮类药物对 BKV-HC 的预防作用。氟喹诺酮类药物在一定程度上可以降低 BK 尿病毒血症的发生率,但可能没有足够的临床效果。